Scientist II - PPT

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)

Job Description

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.

DESCRIPTION:
Join our collaborative R&D team as a Manufacturing Sciences Scientist II, where you'll help solve important challenges in healthcare, environmental protection, and scientific research. In this role, you'll lead the design, development, and optimization of innovative products and processes while working with cross-functional teams to bring new solutions to market. You'll have the opportunity to advance technology through hands-on engineering work, from concept to commercialization, while ensuring compliance with quality standards and regulatory requirements.

You'll contribute to significant projects that directly impact our mission of enabling customers to make the world healthier, cleaner, and safer. You'll apply your technical expertise to solve complex problems, improve existing products, and develop next-generation solutions across our diverse portfolio of scientific instruments and technologies.

REQUIREMENTS:
• Advanced Degree with no prior experience required, OR Bachelor's Degree plus 2 years of experience in GMP manufacturing, process development, or related technical role
• Preferred Fields of Study: Engineering (Mechanical, Electrical, Chemical, Biomedical) or related scientific field
• Strong understanding of cGMP requirements, regulatory compliance, and quality systems
• Experience of design control processes and quality systems (GMP, ISO, FDA requirements)

• Demonstrated ability to analyze technical problems and develop innovative solutions

• Experience in statistical analysis and data interpretation

• Experience with process validation, technology transfer, and scale-up activities
• Excellence in technical documentation and report writing
• Excellent written and verbal communication abilities
• Ability to work independently and collaboratively in a dynamic environment

• Proven track record of meeting project deadlines and deliverables
• Proficient with Microsoft Office Suite and relevant manufacturing/quality systems

• Experience with laboratory instrumentation and analytical techniques
• Experience with risk assessment and root cause analysis
• Ability to train and support team members
• May require occasional weekend/off-hours support
• Must be able to wear required PPE and work in controlled environments
• Physical requirements include ability to lift up to 35 lbs and stand for extended periods

Compensation

The estimated annualized pay range for this position in Ontario is $56,400.00–$84,600.00.